KR890001537A - Uses of 5HT-3 Antagonists - Google Patents

Uses of 5HT-3 Antagonists Download PDF

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KR890001537A
KR890001537A KR1019880008589A KR880008589A KR890001537A KR 890001537 A KR890001537 A KR 890001537A KR 1019880008589 A KR1019880008589 A KR 1019880008589A KR 880008589 A KR880008589 A KR 880008589A KR 890001537 A KR890001537 A KR 890001537A
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임페라또 아순따
뢰머 디트마르
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예안 클라메르
산도즈 리미티드
한스 루돌프 하우스
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Abstract

내용 없음No content

Description

5HT-3 길항제의 용도Uses of 5HT-3 Antagonists

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (32)

1.약물 의존제에 대한 의존도를 방지 또는 감소시키는데 적합한 약물제조에 사용되는 5HT-3 길항제의 용도.1. Use of a 5HT-3 antagonist used in the manufacture of a drug suitable for preventing or reducing dependence on drug dependence. 제1항에 있어서, 5HT-3 길항제는 모느 또는 바이사이클릭 카르복실릭 또느 헤테로사이클릭 카르복실릭산에스테르 도는 아미드 또는 이미다졸릴카르바졸인 것을 특징으로 하는 5HT-3 길항제의 용도.The use of the 5HT-3 antagonist according to claim 1, wherein the 5HT-3 antagonist is all or bicyclic carboxylic or heterocyclic carboxylic acid esters or amides or imidazolylcarbazoles. 정신자극제, 아편이나 알콜 또는 니코틴에 새롭게 의존하는 것을 피하기 위해 약물을 제거한 후 치료하거나 약물의 의존도를 예방 또는 감소시키는데 적합한 약물제조에 사용되는 질소 함유 알콜이나 아민의 모노-또는 바이사이클릭, 카르보사이클릭 또는 헤테로사이클릭 카르복실산에스테르 또는 아미드, 또는 이의 산부가염 또는 4가 암모늄염의 용도.Mono- or bicyclic, carbosai of nitrogen-containing alcohols or amines used in the manufacture of drugs suitable for treatment after drug removal or to prevent or reduce drug dependence in order to avoid new dependence on psychostimulants, opiates or alcohols or nicotine Use of cyclic or heterocyclic carboxylic acid esters or amides, or acid addition salts or tetravalent ammonium salts thereof. 정신자극제의 필요를 감소 또는 방지하거나 정신자극제에 중독된 것을 치료하는데 적합한 의약제조에 사용되는 질소 함유 알콜이나 아민의 모노-또는 바이사이클릭, 카르보사이클릭 또는 헤테로사이클릭 카르복실산에스테르 또는 아미드, 또는 이미다졸릴카르바졸, 또는 이의 산부가염 또는 4가 암모늄염의 용도.Mono- or bicyclic, carbocyclic or heterocyclic carboxylic acid esters or amides of nitrogen-containing alcohols or amines used in the manufacture of a medicament suitable for reducing or preventing the need for a psychostimulant or for treating an addiction to a psychostimulant, Or the use of imidazolylcarbazole, or acid addition salts or tetravalent ammonium salts thereof. 전항 중 어느 한 항에 있어서, 약물 의존제에 대한 의존도를 방지하기 위한 용도.Use according to any one of the preceding claims for preventing dependency on drug dependent agents. 전항 중 어느 한 항에 있어서, 약물 의존제에 대한 의존도를 감소하기 위한 용도.Use according to any one of the preceding claims for reducing dependency on drug dependent agents. 전항 중 어느 한 항에 있어서, 약물 의존제로부터 제거한 후 약물 의존제에 또 다시 의존하는 것을 방지하기 위한 용도.Use according to any one of the preceding claims for preventing the dependence on the drug dependence again after removal from the drug dependence. 전항 중 어느 한 항에 있어서, 약물 의존제는 알콜인 것을 특징으로 하는 용도.Use according to claim 1, wherein the drug dependent agent is an alcohol. 전항 중 어느 한 항에 있어서, 약물 의존제는 니코틴인 것을 특징으로 하는 용도.Use according to any of the preceding claims wherein the drug dependent agent is nicotine. 전항 중 어느 한 항에 있어서, 약물 의존제는 아편인 것을 특징으로 하는 용도.Use according to claim 1, wherein the drug dependent agent is opiate. 전항 중 어느 한 항에 있어서, 약물 의존제는 모르핀인 것을 특징으로 하는 용도.Use according to claim 1, wherein the drug dependent agent is morphine. 전항 중 어느 한 항에 있어서, 약물 의존제는 정신자극제인 것을 특징으로 하는 용도.Use according to any of the preceding claims wherein the drug dependent agent is a psychostimulant. 전항 중 어느 한 항에 있어서, 5HT-3 길항제는 유리 염기형태, 산 부가염형태, 4가 암모늄형태의 하기식(I)의 화합물 또는 하기식(Ia)의 화합물인 것을 특징으로 하는 용도.Use according to any of the preceding claims, characterized in that the 5HT-3 antagonist is a compound of formula (I) or a compound of formula (Ia) in free base form, acid addition salt form, tetravalent ammonium form. A-B-C-DA-B-C-D 상기 식에서 A는 다음 식으로 구성된다.In the above formula, A is composed of the following formula. 상기 식에서 유리 원자가는 식(II,IIa,IIb,IIe 또는 IV)의 링에 부착되어 있으며 ; X-Y는 -CH=CH-, -O=CH2-, 또는 -N-CH-- ; Z는 -CH2-, -NR3-, -O- 또는 -S- ; R1및 R2는 각각 수소, 할로겐, (C1-4)알킬, (C1-4)알콕시, 히드록시, 아미노, (C1-4)알킬아미노, 디(C1-4)알킬아미노, 메르캅토 또는 (C1-4)알킬티오 ; R3는 수소, (C1-4)알킬, 아실, (C3-5)알케닐, 아릴 또는 아릴알킬 ; R4-R7은 각각 수소, 아미노, 니트로, (C1-4)알킬아미노, 디(C1-4)알킬아미노, 할로겐, (C1-4)알콕시, (C1-4)알킬, 알카노일아미노, 피롤릴, 설파모일 또는 카르바모일 ; B는 -CO- 또는 -SO2- ; C는 -O- 또는 -NH- 또는 결합 ; D는 다음 식으로 나타낸다.Wherein the free valence is attached to the ring of formula (II, IIa, IIb, IIe or IV); XY is -CH = CH-, -O = CH 2- , or -N-CH-; Z is -CH 2- , -NR 3- , -O- or -S-; R 1 and R 2 are each hydrogen, halogen, (C 1-4 ) alkyl, (C 1-4 ) alkoxy, hydroxy, amino, (C 1-4 ) alkylamino, di (C 1-4 ) alkylamino , Mercapto or (C 1-4 ) alkylthio; R 3 is hydrogen, (C 1-4 ) alkyl, acyl, (C 3-5 ) alkenyl, aryl or arylalkyl; R 4 -R 7 are each hydrogen, amino, nitro, (C 1-4 ) alkylamino, di (C 1-4 ) alkylamino, halogen, (C 1-4 ) alkoxy, (C 1-4 ) alkyl, Alkanoylamino, pyrrolyl, sulfamoyl or carbamoyl; B is -CO- or -SO 2- ; C is -O- or -NH- or a bond; D is represented by the following formula. [상기 식에서 R8은 수소, (C1-7)알킬, (C3-5)알케닐 또는 알알킬, 식(VIII)에서 결합은 3 또는 4위치에 존재한다] B가 CO일 때 D는 다음 식으로 나타난다.[Wherein R8 is hydrogen, (C 1-7 ) alkyl, (C 3-5 ) alkenyl or alalkyl, the bond in formula (VIII) is at position 3 or 4] When B is CO, D is Appears as [상기 식에서 t는 1 또는 2, R8은 상술한 것과 같다][Wherein t is 1 or 2, R 8 is the same as described above] [상기 식에서 결합은 3(*) 또는 4[*]에 위치한다]Where the bond is at 3 (*) or 4 [*] [상기 식에서 Z는 (C1-4)알콕시][Wherein Z is (C 1-4 ) alkoxy] [상기 식에서, R9-R12는 각각 수소 또는 (C1-4)알킬, m은 0,1 또는 2,n,o,p 또는 각각 0 또는 1]Wherein R 9 -R 12 are each hydrogen or (C 1-4 ) alkyl, m is 0,1 or 2, n, o, p or 0 or 1, respectively] [상기 식에서 q는 2 또는 3 R13및 R14는 각각(C1-4)알킬][Wherein q is 2 or 3 R 13 and R 14 are each (C 1-4 ) alkyl] [상기 식에서 결합은 3 또는 4위치에 존재한다]Where the bond is at the 3 or 4 position [상기 식에서 R8은 상술된 것과 같다][Wherein R 8 is the same as described above] 상기 식에서, R15는 수소, (C1-10)알킬, (C3-9)시클로알킬, (C3-6)알케닐, 페닐 또는 페닐(C1-3)알킬 ; R16, R17또는 R18중 하나는 수소, (C1-6)알킬, (C3-7)시클로알킬, (C2-6)알케닐 또는 페닐(C1-3) 알킬이며 다른 나머지 두 개는 수소, 또는 (C1-4)알킬이다.Wherein R 15 is hydrogen, (C 1-10 ) alkyl, (C 3-9 ) cycloalkyl, (C 3-6 ) alkenyl, phenyl or phenyl (C 1-3 ) alkyl; One of R 16 , R 17 or R 18 is hydrogen, (C 1-6 ) alkyl, (C 3-7 ) cycloalkyl, (C 2-6 ) alkenyl or phenyl (C 1-3 ) alkyl and the other Two are hydrogen or (C 1-4 ) alkyl. 전항 중 어느 한 항에 있어서, 5HT-3 길항제는 유리염기 형태 또는 산부가염 형태의 인돌-3-일-카르복실산 엔도-8-메틸-8-아자바이시클로-[3,2,1]옥토-3-일 에스테르인 용도.The method of claim 1, wherein the 5HT-3 antagonist is indole-3-yl-carboxylic acid endo-8-methyl-8-azabicyclo- [3,2,1] octo in freebase form or in acid addition salt form. Use is a 3-yl ester. 전항 중 어느 한 항에 있어서, 5HT-3 길항제는 유리염기 형태 또는 산부가염 형태의 벤조[b] 티어펜-3-일 카르복실산 엔도-9-메틸-9-아자바이시클로-[3,3,1]-논-3-일 에스테르인 것을 특징으로 하는 용도.The benzo [b] thiophen-3-yl carboxylic acid endo-9-methyl-9-azabicyclo- [3,3] according to any one of the preceding claims, wherein the 5HT-3 antagonist is in free or form acid addition salts. , 1] -non-3-yl ester. 전항 중 어느 한 항에 있어서, 5HT-3 길항제는 유리염기 형태 또는 산부가염 형태의 5-플루오로-1-메틸-인돌-3-일 카르복실산엔도-9-메틸-9-아자바이시클로-[3,3,1]-논-3-일인 것을 특징으로 하는 용도.The 5-HT-3 antagonist according to any one of the preceding claims, 5-fluoro-1-methyl-indol-3-yl carboxylic acid endo-9-methyl-9-azabicyclo in free base form or in acid addition salt form. -[3,3,1] -non-3-yl. 전항 중 어느 한 항에 있어서, 5HT-3 길항제는 1,2,3,9-테트라하이드로-9-메틸-3[(2-메틸-1H-이미다졸-1-일)-메틸]-4H-카르바졸-4-온인 것을 특징으로 하는 용도.The method of claim 1, wherein the 5HT-3 antagonist is 1,2,3,9-tetrahydro-9-methyl-3 [(2-methyl-1H-imidazol-1-yl) -methyl] -4H- Carbazol-4-one. 전항 중 어느 한 항에 있어서, 5HT-3 길항제는 유리염기 형태 또는 산부가염 형태의 엔도-4-아미노-5-클로로-2-메톡시-N-(1-아자바이시클로-[3,3,1]-논-4-일 벤즈아미드인 것을 특징으로 하는 용도.The method of claim 1, wherein the 5HT-3 antagonist is in endo-4-amino-5-chloro-2-methoxy-N- (1-azabicyclo- [3,3, 1] -non-4-yl benzamide. 전항 중 어느 한 항에 있어서, 5HT-3 길항제는 유리염기 형태 또는 산부가염 형태의 1-메틸-인다졸-3-일-카르복실산-9-메틸-아자바이시클로-[3,3,1]-논-3??-알-아미드인 것을 특징으로 하는 용도.The 5HT-3 antagonist of claim 1, wherein the 5HT-3 antagonist is in free base form or in acid addition salt form 1-methyl-indazol-3-yl-carboxylic acid-9-methyl-azabicyclo- [3,3,1 ] -Non-3 ??-al-amide. 전항 중 어느 한 항에 있어서, 5HT-3 길항제는 약물 의존제와 동시에 또는 약물 의존제 투입전에 투여되는 것을 특징으로 하는 용도.Use according to any one of the preceding claims, wherein the 5HT-3 antagonist is administered simultaneously with or prior to the addition of the drug dependent agent. 명세서상에 기재된데로 의존도를 방지 또는 감소시키는데 적합한 의약 제조에 사용되는 5HT-3 길항제의 용도.Use of a 5HT-3 antagonist used in the manufacture of a medicament suitable for preventing or reducing dependence as described in the specification. 전항 중 어느 한 항에서 정의한데로 또는 정의한 방식대로 5HT-3 길항제를 약물 의존도가 높은 환자에게 투여하여 의존도를 방지 또는 감소시키는 방법.A method of preventing or reducing dependence by administering a 5HT-3 antagonist to a patient with high drug dependence as defined in any of the preceding claims or in a defined manner. 전항 중 어느 한 항에서 정의한데로 또는 정의한 방식데로 5HT-3 길항제를 환자에게 투여하여 담배 또는 알콜에 중독되는 것을 감소시키는 방법.A method of reducing addiction to tobacco or alcohol by administering to a patient a 5HT-3 antagonist as defined in any of the preceding claims or in a defined manner. 전항 중 어느 한 항에서 기재한 5HT-3과 약물 의존제의 의존 유도량을 함유하는 것을 특징으로 하는 약학적 조성물.A pharmaceutical composition comprising 5HT-3 as described in any one of the preceding claims and a dependency inducing amount of the drug dependent agent. 5HT-3길항제와 니코틴을 함유하는 것을 특징으로 하는 조성물.A composition comprising 5HT-3 antagonist and nicotine. 0.5-1mg의 5HT-3길항제를 함유하는 경구용 단위용량의 약학적 조성물.An oral unit dose pharmaceutical composition containing 0.5-1 mg of 5HT-3 antagonist. 제26항에 있어서, 길항제는 길항제 자체이거나 제14항에서 정의한 길항제인 것을 특징으로 하는 조성물.27. The composition of claim 26, wherein the antagonist is itself or the antagonist as defined in claim 14. 제26항에 있어서, 길항제는 길항제 자체이거나 제15항에서 정의한 길항제인 것을 특징으로 하는 조성물.The composition of claim 26, wherein the antagonist is itself or the antagonist as defined in claim 15. 제26항에 있어서, 길항제는 길항제 자체이거나 제16항에서 정의한 길항제인 것을 특징으로 하는 조성물.27. The composition of claim 26, wherein the antagonist is itself or the antagonist as defined in claim 16. 제26항에 있어서, 길항제는 길항제 자체이거나 제17항에서 정의한 길항제인 것을 특징으로 하는 조성물.The composition of claim 26, wherein the antagonist is itself or the antagonist as defined in claim 17. 제26항에 있어서, 길항제는 길항제 자체이거나 제18항에서 정의한 길항제인 것을 특징으로 하는 조성물.The composition of claim 26, wherein the antagonist is itself or the antagonist as defined in claim 18. 제26항에 있어서, 길항제는 길항제 자체이거나 제19항에서 정의한 길항제인 것을 특징으로 하는 조성물.The composition of claim 26, wherein the antagonist is itself or the antagonist as defined in claim 19. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임※ Note: The disclosure is based on the initial application.
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JPS6431729A (en) 1989-02-02
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IT1226632B (en) 1991-01-28
FR2617713B1 (en) 1994-08-19
DK385388A (en) 1989-01-12
HU206042B (en) 1992-08-28
PT87958B (en) 1995-03-01
DE3822792C2 (en) 1997-11-27
EP0302008A3 (en) 1992-12-23
MY103536A (en) 1993-07-31
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FR2617713A1 (en) 1989-01-13
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GB2240475B (en) 1992-03-18
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PT87958A (en) 1989-06-30
AU618008B2 (en) 1991-12-12
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